The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
about
Novel alternative splicings of BPAG1 (bullous pemphigoid antigen 1) including the domain structure closely related to MACF (microtubule actin cross-linking factor)Plectin deficiency results in muscular dystrophy with epidermolysis bullosaEnvoplakin, a novel precursor of the cornified envelope that has homology to desmoplakinThe Q-soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Q-SNARE) SNAP-47 Regulates Trafficking of Selected Vesicle-associated Membrane Proteins (VAMPs).Binding of integrin alpha6beta4 to plectin prevents plectin association with F-actin but does not interfere with intermediate filament bindingThe function of intermediate filaments in cell shape and cytoskeletal integrityEvidence for a conformational change in actin induced by fimbrin (N375) bindingMicrotubule actin cross-linking factor (MACF): a hybrid of dystonin and dystrophin that can interact with the actin and microtubule cytoskeletonsAn epidermal plakin that integrates actin and microtubule networks at cellular junctionsPlectin: a cytolinker by designUnique role for the periplakin tail in intermediate filament association: specific binding to keratin 8 and vimentinPlakins: goliaths that link cell junctions and the cytoskeletonThe intermediate filament protein peripherin is the specific interaction partner of mouse BPAG1-n (dystonin) in neuronsHearts of dystonia musculorum mice display normal morphological and histological features but show signs of cardiac stressHerpesvirus tegument protein pUL37 interacts with dystonin/BPAG1 to promote capsid transport on microtubules during egress.GAS2-like proteins mediate communication between microtubules and actin through interactions with end-binding proteins.Central serotonin system in Dystonia musculorum mutant mice: biochemical, autoradiographic and immunocytochemical data.An induction gene trap for identifying a homeoprotein-regulated locus.Serum anti-BPAG1 auto-antibody is a novel marker for human melanomaInteraptin, an actin-binding protein of the alpha-actinin superfamily in Dictyostelium discoideum, is developmentally and cAMP-regulated and associates with intracellular membrane compartments.Nervous-tissue-specific elimination of microtubule-actin crosslinking factor 1a results in multiple developmental defects in the mouse brain.Animal models of generalized dystonia.Motor unit abnormalities in Dystonia musculorum miceCollagen XVII and BPAG1 expression in the retina: evidence for an anchoring complex in the central nervous system.Epiplakin is dispensable for skin barrier function and for integrity of keratin network cytoarchitecture in simple and stratified epithelia.The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.Dyshidrosiform pemphigoid with Parkinsonism in a nonagenarian Maharashtrian female.Neuronal degeneration in autonomic nervous system of Dystonia musculorum mice.Untethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunctionA population-based study of the association between bullous pemphigoid and neurologic disorders.Periplakin gene targeting reveals a constituent of the cornified cell envelope dispensable for normal mouse development.Interaction of the bullous pemphigoid antigen 1 (BP230) and desmoplakin with intermediate filaments is mediated by distinct sequences within their COOH terminus.Animal models of dystonia: Lessons from a mutant rat.Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function.Microtubule stability, Golgi organization, and transport flux require dystonin-a2-MAP1B interaction.The role of the laboratory mouse in the human genome projectThe beta-globin locus control region enhances transcription of but does not confer position-independent expression onto the lacZ gene in transgenic mice.Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS MyelinationSpectraplakins: master orchestrators of cytoskeletal dynamics.Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice.
P2860
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P2860
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
description
1995 nî lūn-bûn
@nan
1995 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@ast
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@en
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@nl
type
label
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@ast
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@en
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@nl
prefLabel
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@ast
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@en
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@nl
P2093
P2860
P356
P1433
P1476
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
@en
P2093
P2860
P2888
P304
P356
10.1038/NG0795-301
P407
P577
1995-07-01T00:00:00Z
P5875
P6179
1030951123